Canonical Allele Identifier: CA363509935
Gene: AGER HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32181388T>G , CM000668.2:g.32181388T>G GRCh38
NC_000006.11:g.32149165T>G , CM000668.1:g.32149165T>G GRCh37
NC_000006.10:g.32257143T>G NCBI36
NG_029868.1:g.7935A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000375076.9:c.1081A>C MANE Select ENSP00000364217.4:p.Ile361Leu
ENST00000375055.6:c.*29+136A>C ENSP00000364195.2:n.*29+136A>C
ENST00000375065.6:c.268A>C ENSP00000364206.6:p.Ile90Leu
ENST00000375067.7:c.926A>C ENSP00000364208.3:p.His309Pro
ENST00000375069.7:c.1129A>C ENSP00000364210.4:p.Ile377Leu
ENST00000375070.7:c.751A>C ENSP00000364211.4:p.Ile251Leu
ENST00000375076.8:c.1081A>C ENSP00000364217.4:p.Ile361Leu
ENST00000438221.6:c.*29+136A>C ENSP00000387887.2:n.*29+136A>C
ENST00000469940.5:n.248A>C
ENST00000473619.5:n.623A>C
ENST00000484849.5:n.1288A>C
ENST00000488669.5:n.615+136A>C
ENST00000620802.4:c.328A>C ENSP00000484081.1:p.Ile110Leu
NM_001136.4:c.1081A>C NP_001127.1:p.Ile361Leu
NM_001206929.1:c.1129A>C NP_001193858.1:p.Ile377Leu
NM_001206932.1:c.1039A>C NP_001193861.1:p.Ile347Leu
NM_001206934.1:c.*29+136A>C NP_001193863.1:n.*29+136A>C
NM_001206936.1:c.1021+136A>C NP_001193865.1:n.1021+136A>C
NM_001206940.1:c.*29+136A>C NP_001193869.1:n.*29+136A>C
NM_001206954.1:c.931+136A>C NP_001193883.1:n.931+136A>C
NM_001206966.1:c.*29+136A>C NP_001193895.1:n.*29+136A>C
NM_172197.2:c.926A>C NP_751947.1:p.His309Pro
NR_038190.1:n.1364A>C
XM_017010328.2:c.1072+136A>C XP_016865817.1:n.1072+136A>C
XR_001743189.2:n.1145A>C
XR_001743190.2:n.1097A>C
NM_001136.5:c.1081A>C MANE Select NP_001127.1:p.Ile361Leu
NM_001206932.2:c.1039A>C NP_001193861.1:p.Ile347Leu
NM_001206936.2:c.1021+136A>C NP_001193865.1:n.1021+136A>C
NM_001206940.2:c.*29+136A>C NP_001193869.1:n.*29+136A>C
NM_001206954.2:c.931+136A>C NP_001193883.1:n.931+136A>C
NM_001206966.2:c.*29+136A>C NP_001193895.1:n.*29+136A>C
NM_172197.3:c.926A>C NP_751947.1:p.His309Pro
NR_038190.2:n.1295A>C
NM_001206929.2:c.1129A>C NP_001193858.1:p.Ile377Leu
NM_001206934.2:c.*29+136A>C NP_001193863.1:n.*29+136A>C